drugset / Trial / NCT02928029

Study Testing Radium-223 Dichloride in Relapsed Multiple Myeloma

NCT02928029

Phase 1/2 Terminated 7 enrolled Bayer
RandomizedSequentialQuadruple-blindTreatment

Summary

This study will be conducted in 2 parts. The phase 1b part will be an international, phase 1b, open-label, dose-escalation assessment of radium-223 dichloride administered with bortezomib and dexamethasone in subjects with relapsed multiple myeloma. The primary endpoint is to determine the optimal dose of radium-223 dichloride in combination with bortezomib/dexamethasone for the Phase 2 portion of the study. The phase 2 part will be an international, phase 2, double-blind, randomized, placebo-controlled assessment of radium-223 dichloride versus placebo administered with bortezomib and dexamethasone, in subjects with relapsed multiple myeloma. Up to 12 subjects in all dose cohorts combined will be treated in the phase 1b part of the study. Up to approximately 100 subjects will be enrolled in the phase 2 part of the study.

Timeline

Start
2017-02-10
Primary completion
2019-03-20
Completion
2019-03-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Radium-223 dichloride Other / unclassified 0.033 mbq/kg Intravenous
Subject Radium-223 dichloride Other / unclassified 0.055 mbq/kg Intravenous
Background Bortezomib Small molecule 1.3 mg/m2 Subcutaneous
Background Dexamethasone Small molecule 40 mg Oral

Indications